Epst Homo NDC 43742-2173

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2173Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2173Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43742-2173-1	43742217301	30 mL in 1 BOTTLE, DROPPER (43742-2173-1)Marketed from Aug 15, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Epst Homo
Generic name (nonproprietary): epstein-barr virus dna, epstein-barr virus nosode
Active ingredients: Herring sperm DNA — 15 [hp_C]/mLHuman herpesvirus 4 — 15 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2173_b617bcc1-2187-4296-8900-23968b492d4aSPL ID b617bcc1-2187-4296-8900-23968b492d4aSPL set ID 8fa536b9-a2a2-4055-a09b-a10ce4546f61UNII 51FI676N6F, 2A26YW7PNXUPC 0810151882826

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742217301 followed by a unit qualifier and the quantity

Package 43742-2173-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Apr 8, 2025.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • exhaustion • mucus congestion • fatigue These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)